Other mutations in this stock |
Total: 35 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310033P09Rik |
A |
G |
11: 59,099,674 (GRCm39) |
T92A |
probably damaging |
Het |
Ankhd1 |
A |
G |
18: 36,765,125 (GRCm39) |
S1007G |
probably benign |
Het |
Cabp4 |
A |
T |
19: 4,189,406 (GRCm39) |
S50R |
possibly damaging |
Het |
Camp |
A |
T |
9: 109,678,336 (GRCm39) |
L56Q |
probably damaging |
Het |
Cblb |
A |
G |
16: 51,986,461 (GRCm39) |
N568S |
probably benign |
Het |
Ccr6 |
C |
A |
17: 8,474,825 (GRCm39) |
T10K |
probably benign |
Het |
Chit1 |
T |
C |
1: 134,072,992 (GRCm39) |
F106S |
probably damaging |
Het |
Cyb561d1 |
A |
G |
3: 108,106,943 (GRCm39) |
L34P |
probably damaging |
Het |
Dcun1d1 |
A |
T |
3: 35,975,114 (GRCm39) |
|
probably benign |
Het |
Deup1 |
A |
G |
9: 15,521,967 (GRCm39) |
|
probably benign |
Het |
Erich1 |
A |
G |
8: 14,083,518 (GRCm39) |
F184S |
probably damaging |
Het |
Fmnl3 |
A |
G |
15: 99,235,509 (GRCm39) |
|
probably null |
Het |
Grk2 |
T |
C |
19: 4,337,982 (GRCm39) |
N508S |
probably benign |
Het |
Herc4 |
A |
G |
10: 63,109,316 (GRCm39) |
I184V |
probably benign |
Het |
Hnrnpm |
C |
A |
17: 33,868,876 (GRCm39) |
R517L |
probably damaging |
Het |
Ift56 |
T |
C |
6: 38,359,155 (GRCm39) |
|
probably benign |
Het |
Kif3b |
G |
A |
2: 153,158,381 (GRCm39) |
A61T |
possibly damaging |
Het |
Kmt2d |
G |
A |
15: 98,742,890 (GRCm39) |
|
probably benign |
Het |
Lrrc7 |
C |
A |
3: 157,866,727 (GRCm39) |
V1005L |
possibly damaging |
Het |
Lrrtm1 |
A |
T |
6: 77,221,046 (GRCm39) |
M168L |
probably benign |
Het |
Ndc1 |
C |
T |
4: 107,241,977 (GRCm39) |
|
probably benign |
Het |
Nphs1 |
A |
G |
7: 30,160,164 (GRCm39) |
|
probably benign |
Het |
Or52w1 |
A |
T |
7: 105,018,454 (GRCm39) |
Y298F |
probably damaging |
Het |
Pbld2 |
T |
C |
10: 62,907,734 (GRCm39) |
V200A |
probably benign |
Het |
Pcdhb21 |
A |
G |
18: 37,647,606 (GRCm39) |
Y245C |
probably damaging |
Het |
Pcm1 |
A |
G |
8: 41,740,918 (GRCm39) |
T1055A |
probably damaging |
Het |
Plcl2 |
C |
T |
17: 50,913,948 (GRCm39) |
S319L |
probably benign |
Het |
Plekha8 |
C |
A |
6: 54,606,822 (GRCm39) |
Y372* |
probably null |
Het |
Ralb |
T |
A |
1: 119,399,506 (GRCm39) |
N184I |
probably benign |
Het |
Robo3 |
C |
T |
9: 37,339,050 (GRCm39) |
|
probably null |
Het |
Slc41a1 |
T |
A |
1: 131,766,914 (GRCm39) |
L144H |
probably damaging |
Het |
Smg1 |
C |
T |
7: 117,739,855 (GRCm39) |
G3364D |
probably damaging |
Het |
Spmap2 |
A |
G |
10: 79,412,433 (GRCm39) |
S329P |
probably damaging |
Het |
Zbtb7c |
T |
C |
18: 76,278,921 (GRCm39) |
S460P |
possibly damaging |
Het |
Zscan30 |
T |
C |
18: 24,104,834 (GRCm39) |
|
noncoding transcript |
Het |
|
Other mutations in Vmn1r123 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02330:Vmn1r123
|
APN |
7 |
20,896,969 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02742:Vmn1r123
|
APN |
7 |
20,896,968 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL03240:Vmn1r123
|
APN |
7 |
20,896,282 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1173:Vmn1r123
|
UTSW |
7 |
20,896,257 (GRCm39) |
missense |
probably damaging |
0.99 |
R6278:Vmn1r123
|
UTSW |
7 |
20,896,774 (GRCm39) |
missense |
possibly damaging |
0.78 |
R6610:Vmn1r123
|
UTSW |
7 |
20,896,515 (GRCm39) |
missense |
probably benign |
0.00 |
R6679:Vmn1r123
|
UTSW |
7 |
20,896,868 (GRCm39) |
nonsense |
probably null |
|
R7241:Vmn1r123
|
UTSW |
7 |
20,896,537 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7642:Vmn1r123
|
UTSW |
7 |
20,896,795 (GRCm39) |
missense |
probably benign |
0.11 |
R7702:Vmn1r123
|
UTSW |
7 |
20,896,302 (GRCm39) |
missense |
probably damaging |
0.99 |
R7870:Vmn1r123
|
UTSW |
7 |
20,896,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R7981:Vmn1r123
|
UTSW |
7 |
20,896,914 (GRCm39) |
missense |
probably damaging |
0.98 |
R8554:Vmn1r123
|
UTSW |
7 |
20,896,971 (GRCm39) |
missense |
probably benign |
|
R9079:Vmn1r123
|
UTSW |
7 |
20,896,979 (GRCm39) |
missense |
probably benign |
0.01 |
R9090:Vmn1r123
|
UTSW |
7 |
20,896,794 (GRCm39) |
missense |
probably benign |
|
R9271:Vmn1r123
|
UTSW |
7 |
20,896,794 (GRCm39) |
missense |
probably benign |
|
R9544:Vmn1r123
|
UTSW |
7 |
20,896,987 (GRCm39) |
missense |
probably benign |
0.30 |
R9779:Vmn1r123
|
UTSW |
7 |
20,896,111 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
|